Solving a 50 year mystery of a missing OPA1 mutation: more insights from the first family diagnosed with autosomal dominant optic atrophy

por Fuhrmann, Nico, Schimpf, Simone, Kamenisch, York, Leo-Kottler, Beate, Alexander, Christiane, Auburger, Georg, Zrenner, Eberhart, Wissinger, Bernd, Alavi, Marcel V
Publicado 2010

Proteins of nucleotide and base excision repair pathways interact in mitochondria to protect from loss of subcutaneous fat, a hallmark of aging

por Kamenisch, York, Fousteri, Maria, Knoch, Jennifer, von Thaler, Anna-Katharina, Fehrenbacher, Birgit, Kato, Hiroki, Becker, Thomas, Dollé, Martijn E.T., Kuiper, Raoul, Majora, Marc, Schaller, Martin, van der Horst, Gijsbertus T.J., van Steeg, Harry, Röcken, Martin, Rapaport, Doron, Krutmann, Jean, Mullenders, Leon H., Berneburg, Mark
Publicado 2010